2-Piperidino-4-imino-2-thiazoline hydrochloride → HCID 178436237, 화합물

HRID 1112536노트

반응식

HRID 1112536 반응식
[CH2:1]([C:3]1[C:11]([CH2:12][CH3:13])=[C:10]([CH2:14][CH3:15])[C:9]([CH2:16][CH3:17])=[C:8]2[C:4]=1[C:5](=[NH:19])[NH:6][C:7]2=N)[CH3:2].[ClH:20].[CH:21]([NH:24][C:25]1[S:26][CH2:27][C:28](=[NH:30])[N:29]=1)([CH3:23])[CH3:22].N=C1C2C(=CC=CC=2)C(=N)N1.Cl.N1(C2SCC(=N)N=2)CCCCC1>>[ClH:20].[NH:19]=[C:5]1[C:4]2[C:8](=[C:9]([CH2:16][CH3:17])[C:10]([CH2:14][CH3:15])=[C:11]([CH2:12][CH3:13])[C:3]=2[CH2:1][CH3:2])[C:7](=[C:27]2[S:26][C:25]([NH:24][CH:21]([CH3:23])[CH3:22])=[N:29][C:28]2=[NH:30])[NH:6]1

참가 물질

5

반응물 4

HCID 162452962-Piperidino-4-imino-2-thiazoline hydrochlorideHCID 178436238HCID 178436238, 화합물HCID 178456873HCID 178456873, 화합물HCID 178508669HCID 178508669, 화합물

생성물 1

HCID 178436237HCID 178436237, 화합물

실험 절차

When equivalent amounts of 4,5,6,7-tetraethyl-1,3-diiminoisoindoline and 2-isopropylamino-4-imino-2-thiazoline hydrochloride are substituted for the 1,3-diiminoisoindoline and 2-piperidino-4-imino-2-thiazoline hydrochloride respectively, in the procedure described in Example 9, part B above, there is obtained as the product 1-imino-4,5,6,7-tetraethyl-3-(2-isopropylamino-4-imino-2-thiazolin-5-ylidene)isoindoline hydrochloride.

출처 및 근거

ORD 기록
ord-4e55c37a94ff43938663c408b6b3bf33
출처 데이터셋
uspto-grants-1978_10
특허 번호
US04122261

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