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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 86661313, 화합물

HRID 1685079
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HRID 1685079 반응식
CP(C)C.[N:5]([CH2:8][C:9]1[N:10]=[C:11]([NH:14][C:15]([NH:17][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[C:21]([F:25])[CH:20]=2)=[O:16])[S:12][CH:13]=1)=[N+]=[N-].[ClH:26]>C1COCC1>[ClH:26].[NH2:5][CH2:8][C:9]1[N:10]=[C:11]([NH:14][C:15]([NH:17][CH2:18][C:19]2[CH:24]=[CH:23][CH:22]=[C:21]([F:25])[CH:20]=2)=[O:16])[S:12][CH:13]=1
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 68983TrimethylphosphineHCID 86661312HCID 86661312, 화합물

생성물 1

HCID 86661313HCID 86661313, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Trimethylphosphine (107 μL, 1.2 mmol) was added dropwise to a THF (5 mL) solution of 1-(4-(azidomethyl)thiazol-2-yl)-3-(3-fluorobenzyl)urea (307 mg, 1.0 mmol) at 0 C under a nitrogen atmosphere. The mixture was stirred for 22 hours then HCl (0.5 mL, 4M in water) was added and the stirring was continued for 22 hours. Upon evaporation of the mixture, the product was recrystallized from acetonitrile to afford 1-(4-(aminomethyl) thiazol-2-yl)-3-(3-fluorobenzyl)urea hydrochloride. 1H NMR (400 MHz, CD3OD): δ 10.3 (1H, br), 7.34 (m, 1H), 7.17-6.95 (m, 4H), 4.45 (s, 2H), 4.08 (s, 2H). MS (ES+): M/Z 281 (M+H)+.

후처리

  1. waitthe stirring was continued for 22 hours
  2. customUpon evaporation of the mixture
  3. customthe product was recrystallized from acetonitrile

출처 및 근거

ORD 기록
ord-792c87b0ea1d4ef0b097960fcb9390d3
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08148380B2

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