Hydrochloric Acid → phenyl 3-(1-methyl-1H-tetraazol-5-yl)phenylcarbamate

HRID 1169204ノート

反応式

HRID 1169204 の反応式
[CH3:1][N:2]1[C:6]([C:7]2[CH:12]=[CH:11][CH:10]=[C:9]([NH2:13])[CH:8]=2)=[N:5][N:4]=[N:3]1.N1C(C)=CC=CC=1C.Cl[C:23]([O:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)=[O:24].Cl>ClCCl>[C:26]1([O:25][C:23](=[O:24])[NH:13][C:9]2[CH:10]=[CH:11][CH:12]=[C:7]([C:6]3[N:2]([CH3:1])[N:3]=[N:4][N:5]=3)[CH:8]=2)[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 79372,6-LutidineHCID 15891Phenyl chloroformateHCID 144576753-(1-methyl-1H-1,2,3,4-tetrazol-5-yl)aniline

生成物 1

HCID 22252681phenyl 3-(1-methyl-1H-tetraazol-5-yl)phenylcarbamate収率 84.9%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

In a dry flask of 1-methyl-5-(3-aminophenyl)-tetrazole (24.0 g, 137 mmol) was dissolved in dichloromethane (1.4 L) and 2,6-lutidine (44.1 g, 411 mmol) was added. Phenyl chloroformate (21.2 g, 136 mmol) was added in 4 portions over 15 minutes, then the reaction was stirred for 1.5 hours. The reaction was poured into 1N aqueous hydrochloric acid (200 mL) and the mixture was extracted with dichloromethane three times (200 mL). The combined organic layers were washed with brine, dried with sodium sulfate, filtered, and concentrated in vacuo. The crude brown material was dissolved in hot toluene, filtered, and allowed to precipitate at 0° C. to give 34.1 g of a white solid. The filtrate was concentrated and recrystallized from toluene again to give an additional crop of off-white crystals (3.44 g, 93% total). 1H NMR (300 MHz, CDCl3), δ: 10.51 (bs, 1H), 8.01 (s, 1H), 7.71 (dt, J=7, J′=2, 1H), 7.55 (m, 2H), 7.41 (m, 2H), 7.24 (m, 2H), 4.14 (s, 3H).

後処理

  1. extractionthe mixture was extracted with dichloromethane three times (200 mL)
  2. washThe combined organic layers were washed with brine
  3. dry with materialdried with sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. dissolutionThe crude brown material was dissolved in hot toluene
  7. filtrationfiltered
  8. customto precipitate at 0° C.

出典と根拠

ORDレコード
ord-f1db3acd64be4e88b19f1e2baecef867
出典データセット
uspto-grants-2003_09
特許番号
US06627629B2

反応ノート

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