HCID 22764174, compound → HCID 178421876, compound

HRID 1112548Notes

Reaction equation

HRID 1112548 reaction equation
[Br:1][CH:2]1[CH2:10][CH:9]([CH3:11])[CH2:8][C:7]2[C:6](=[NH:12])[NH:5][C:4](=N)[C:3]1=2.Cl.[CH3:15][CH:16]1[CH2:21][N:20]([C:22]2[S:23][CH2:24][C:25](=[NH:27])[N:26]=2)[CH2:19][CH2:18][O:17]1.N=C1C2CCCCC=2C(=N)N1.Cl.N=C1NC(=N)CS1>>[NH:12]=[C:6]1[C:7]2[CH2:8][CH:9]([CH3:11])[CH2:10][CH:2]([Br:1])[C:3]=2[C:4](=[C:24]2[S:23][C:22]([N:20]3[CH2:19][CH2:18][O:17][CH:16]([CH3:15])[CH2:21]3)=[N:26][C:25]2=[NH:27])[NH:5]1

Participants

5

Reactant 4

HCID 22764174HCID 22764174, compoundHCID 176526843HCID 176526843, compoundHCID 178422102HCID 178422102, compoundHCID 178479111HCID 178479111, compound

Product 1

HCID 178421876HCID 178421876, compound

Procedure

Proceeding in a manner similar to that described above in Example 10, part A, but substituting equivalent amounts of 4-bromo-6-methyl-4,5,6,7-tetrahydro-1,3-diiminoisoindoline and 2-(2-methylmorpholino)-4-imino-2-thiazoline hydrochloride for 4,5,6,7-tetrahydro-1,3-diiminoisoindoline and 2,4-diiminothiazolidine hydrochloride respectively, there is obtained as the product 1-imino-4-bromo-6-methyl-4,5,6,7-tetrahydro-3-[2-(2-methylmorpholino)-4-imino-2-thiazolin-5-ylidene]isoindoline.

Sources & evidence

ORD record
ord-889c6df9973b4c36b1ce1912f94f0677
Source dataset
uspto-grants-1978_10
Patent number
US04122261

Reaction notes

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