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Acetic Acid → HCID 21714707, 화합물

HRID 650253
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인쇄 미리보기

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HRID 650253 반응식
C([BH3-])#N.[Na+].[C:5]([C:9]1[CH:14]=[CH:13][C:12]([CH2:15][CH:16]([CH3:20])[CH2:17][NH:18][CH3:19])=[CH:11][CH:10]=1)([CH3:8])([CH3:7])[CH3:6].[CH:21]([C:23]1[CH:24]=[N:25][N:26]([CH3:28])[CH:27]=1)=O.C(O)(=O)C>CO>[C:5]([C:9]1[CH:10]=[CH:11][C:12]([CH2:15][CH:16]([CH3:20])[CH2:17][N:18]([CH2:21][C:23]2[CH:24]=[N:25][N:26]([CH3:28])[CH:27]=2)[CH3:19])=[CH:13][CH:14]=1)([CH3:8])([CH3:6])[CH3:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 5731171-Methyl-1H-pyrazole-4-carbaldehydeHCID 5003444Sodium cyanoborohydrideHCID 13787913110135-01-8

생성물 1

HCID 21714707HCID 21714707, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Route B-2: After suspending 200 mg (3.2 mmol) of sodium cyanoborohydride in 2 ml of absolute methanol, 380 mg (1.7 mmol) of 3-(4-t-butylphenyl)-N,2-dimethylpropylamine (IV-1) was added thereto. Subsequently, to this was added a solution of 170 mg (1.6 mmol) 4-formyl-1-methylpyrazole/2 ml absolute methanol by portions, the pH was adjusted to 7 with acetic acid, and then stirring was conducted at room temperature for 8 h.

후처리

  1. additionwas added

출처 및 근거

ORD 기록
ord-0682b80bd99c441abcc53ac55187fffd
출처 데이터셋
uspto-grants-2001_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06271385B1

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